Cannabinoid Receptors and Novel Antiglaucoma Drugs

大麻素受体和新型抗青光眼药物

• 批准号: 7655084
• 负责人: ZHAO-HUI SONG
• 金额: $ 37万
• 依托单位: UNIVERSITY OF LOUISVILLE
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-08-01 至 2011-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7655084
• 关键词: Address; Agonist; Animal Model; Anterior; Anti-glaucoma Agent; Aqueous Humor; Biological Assay; Blindness; CNR2 gene; Cannabinoids; Cells; Development; Funding; GTP Binding; Glaucoma; Homeostasis; Immunohistochemistry; Lead; Marijuana; Matrix Metalloproteinases; Mediating; Metalloproteases; Optic Nerve; Physiologic Intraocular Pressure; Play; Risk Factors; Role; Signal Transduction; Testing; Therapeutic Agents; Trabecular meshwork structure; Western Blotting; antiglaucoma drug; cannabinoid receptor; design; human subject; insight; novel; research study

Glaucoma is one of the leading causes of blindness worldwide. Elevated intraocular pressure (IOP) is the primary risk factor for optic nerve damage in glaucoma. Many studies conducted on human subjects and animal models have shown that marijuana and its active components cannabinoids lower IOP. This project is focused on understanding the mechanisms by which cannabinoids, potential therapeutic agents for glaucoma, lower intraocular pressure (IOP). In the previous funding period, we have established that CB1 and CB2 cannabinoid receptors are expressed on the trabecular meshwork (TM) cells, and cannabinoid agonists enhance aqueous humor outflow through both CB1 and CB2 receptors. For the competitive renewal application of this project, we hypothesize that non-CB1/CB2 cannabinoid derivatives may cause an enhancement of aqueous humor outflow through a novel, non-CB1/CB2 cannabinoid receptor, and the novel cannabinoid receptor may mediates the IOP-lowering effects of the non-CB1/CB2 cannabinoid agonists through metalloprotease (MMP)-mediated mechanisms. Two specific aims are designed to test the above three hypotheses. Specific Aim 1: To study the effects of non-CB1/CB2 cannabinoid agonists, and the role of GPR55, a novel, non- CB1/CB2 cannabinoid receptor on aqueous humor outflow. Specific Aim 2: To study the mechanisms of actions for the aqueous humor outflow-enhancing effects of non-CB1/CB2 cannabinoid agonists. Completing this project should provide mechanistic insight regarding cannabinoid-induced enhancement of aqueous humor outflow facility. These studies should also contribute to our understanding of the homeostasis of aqueous humor outflow and may lead to the development of better therapeutic agents for lowering IOP.

青光眼是全世界导致失明的主要原因之一。眼压（IOP）升高是主要风险 青光眼视神经损伤的因素。对人类受试者和动物模型进行的许多研究表明 大麻及其活性成分大麻素可降低眼压。该项目的重点是了解 大麻素（青光眼的潜在治疗剂）降低眼内压（IOP）的机制。在 在之前的资助期间，我们已经确定 CB1 和 CB2 大麻素受体在小梁上表达 网状细胞 (TM) 和大麻素激动剂通过 CB1 和 CB2 受体增强房水流出。 对于本项目的竞争性续展申请，我们假设非CB1/CB2大麻素衍生物可能 通过新型非 CB1/CB2 大麻素受体引起房水流出增强，并且新型 大麻素受体可能通过非 CB1/CB2 大麻素激动剂介导降低眼压的作用 金属蛋白酶（MMP）介导的机制。设计了两个具体目标来检验上述三个假设。 具体目标 1：研究非 CB1/CB2 大麻素激动剂的作用，以及 GPR55（一种新型非 CB1/CB2 大麻素受体对房水流出。具体目标 2：研究作用机制 非 CB1/CB2 大麻素激动剂的房水流出增强作用。完成该项目应提供 关于大麻素诱导的房水流出设施增强的机制见解。这些研究应该 也有助于我们了解房水流出的稳态，并可能导致 更好的降低眼压的治疗药物。